FDA 510(k) Applications Submitted by PDO MAX, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190245 | 02/06/2019 | PDS Barbed Suture, PDO MAXX Threads | PDO MAX, Inc. |
| K210871 | 03/24/2021 | PDO Max Suture with Dual Needle | PDO MAX, Inc. |
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